A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18151166



Internal ID20718206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:121094201..121096700hg38UCSC Ensembl
chr7:120734255..120736754hg19UCSC Ensembl
Cytoband7q31.31
Allele length
AssemblyAllele length
hg382500
hg192500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6607910
Supporting Variants
Samples
Known GenesCPED1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18151166
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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